Table 1.

Genomic findings

Gene/genomic location	Chr	HGVS DNA ref	HGVS protein ref	Variant type	Predicted effect	Allele frequency	Target coverage
ALK	2	t(2;2)(p23;p21)(hg19 Chr 2:g.42552694::oChr 2:g.29446394)	n/a	EML4–ALK fusion	Oncogenic	n/a	301×